Tip-based photoemission
spectroscopic techniques have now achieved
subnanometer resolution that allows visualization of the chemical
structure and even the ground-state vibrational modes of a single
molecule. However, the ability to visualize the interplay between
electronic and nuclear motions of excited states, i.e., vibronic couplings,
is yet to be explored. Herein, we theoretically propose a new technique,
namely, tip-enhanced fluorescence excitation (TEFE). TEFE takes advantage
of the highly confined plasmonic field and thus can offer a possibility
to directly visualize the vibronic effect of a single molecule in
real space for arbitrary excited states in a given energy window.
Numerical simulations for a single porphine molecule confirm that
vibronic couplings originating from Herzberg–Teller (HT) active
modes can be visually identified. TEFE further enables high-order
vibrational transitions that are normally suppressed in the other
plasmon-based processes. Images of the combination vibrational transitions
have the same pattern as that of their parental HT active mode’s
fundamental transition, providing a direct protocol for measurements
of the activity of Franck–Condon modes of selected excited
states. These findings strongly suggest that TEFE is a powerful strategy
to identify the involvement of molecular moieties in the complicated
electron–nuclear interactions of the excited states at the
single-molecule level.